Top 9 Process validation associate iii Jobs in Bloomington, In

Process Validation Associate III
Simtra BioPharma Solutions —Bloomington, IN
- Overtime
- Microsoft Excel
- Microsoft Outlook
- Computer literacy
- Paid parental leave
- AD&D insurance
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Quality Engineer III
Boston Scientific —Spencer, IN
- $74,600 - $141,700 a year
- Engineering
- Neurology
- Mentoring
Aseptic Manufacturing Risk Management Associate II
Simtra BioPharma Solutions —Bloomington, IN
- Overtime
- Microsoft Excel
- Microsoft Outlook
- Computer literacy
- Paid parental leave
- AD&D insurance
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MSAT Senior Associate (Tech Transfer)
Simtra BioPharma Solutions —Bloomington, IN
- Overtime
- Microsoft Excel
- Microsoft Outlook
- Computer literacy
- Paid parental leave
- AD&D insurance
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Packaging Validation Associate I - 1st Shift
Simtra BioPharma Solutions —Bloomington, IN
- Overtime
- Microsoft Excel
- Microsoft Outlook
- Engineering
- Paid parental leave
- AD&D insurance
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Sterility Assurance Validation Associate I (1st shift)
Simtra BioPharma Solutions —Bloomington, IN
- Overtime
- Microsoft Excel
- 6 years
- Microsoft Outlook
- Paid parental leave
- AD&D insurance
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Process Validation Associate III

Simtra BioPharma Solutions -
Bloomington, IN

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Job Details

Benefits

Paid parental leave
AD&D insurance
Paid holidays
Disability insurance
Health insurance
Dental insurance
Flexible spending account
Paid time off
Adoption assistance
Parental leave
Employee assistance program
Vision insurance
401(k) matching
Benefits from day one
Life insurance

Qualifications

Microsoft Excel
Microsoft Outlook
Cleanroom protocols
Manufacturing facility experience
Bachelor's degree
Continuous improvement
Pharmaceutical company experience
Sterile attire donning
Cleanroom experience
Technical Proficiency
Pharmaceutical manufacturing facility experience

Full Job Description

Simtra BioPharma Solutions (Simtra) is a world-class Contract Development Manufacturing Organization, partnering with pharmaceutical and biotech companies to bring their sterile injectable products to market. With facilities in Bloomington, Indiana, US and Halle/Westfalen, Germany, we offer a wide range of delivery systems including pre-filled syringes, liquid/lyophilized vials, diluents for reconstitution, powder-filled vials and sterile crystallization.

Our product types include biologics and small molecules, cytotoxics, highly potent compounds, diluents for reconstitution and vaccines – which are all directly injected into patients worldwide. As such, there is a strong emphasis on quality and continuous improvement at Simtra. We hold ourselves to the highest quality and regulatory standards.

While our primary focus is cGMP manufacturing, we offer many support services including formulation and development, lyophilization optimization, global regulatory support and secondary packaging. Our teams are driven to help clients scale, innovate and bring life-changing medicines to patients worldwide.

Why join Team Simtra? Because we:

Make it HAPPEN – We bring a growth mindset to every opportunity, developing new skillsets and exceeding our expectations and those of our customers.

Make it TOGETHER – We work as one, respecting each voice and tapping into our unique strengths across teams—so we can solve problems in new ways.

Make it RIGHT – We hold ourselves to a high standard of excellence, fulfilling our commitments to the customer, their patients, and our team members.

Make it COUNT – We take pride in our day-to-day work, knowing the impact we make – taking on challenges big and small to improve patient health.

The role:

This position executes process validation activities that meet worldwide regulatory agency requirements, internal company standards/best practices and current industry practices. This position interacts with the client and the cross functional client team members to develop process validation strategies and creates process validation protocol and summary documents. This position reports to the Process Validation Sr. Manager.

The responsibilities:

Support and maintain the process validation program.
Develop, revise, and maintain process validation procedures, protocols, and summary reports.
Partner with clients and internal teams to define validation scope, requirements, and objectives.
Design, execute, and analyze technical studies using statistical tools to establish and evaluate process parameters.
Perform risk assessments to support process validation activities.
Plan, coordinate, and execute process validation activities for new and existing products.
Analyze validation data and prepare documentation to support validation conclusions.
Conduct annual reviews and Continued Process Verification (CPV) activities to ensure ongoing process performance.
Lead or support investigations related to validation activities, including Non-Conformance Reports (NCRs) and Corrective and Preventive Actions (CAPAs).
Monitor regulatory requirements and industry best practices to ensure compliance and continuous improvement.
Create and maintain visual management tools and controls for the Process Validation group.
Serve as a Subject Matter Expert (SME) for process validation during regulatory, client, and internal audits.
Develop industry expertise and project proficiency while working independently on assigned initiatives.
Identify and implement opportunities to optimize departmental processes and improve operational efficiency.

Required qualifications:

Bachelor's degree required, preferably in a science or engineering-related field.
Minimum of 5 years of technical experience (validation preferred) in parenteral manufacturing.
Computer proficiency in Microsoft Word, Excel, and Outlook and the ability to use enterprise software (examples include: JDE, BPLM, Pilgrim, Trackwise, etc.).
Ability to communicate effectively at all levels.
Sound industry knowledge, project proficiency, and be able to work independently. May be considered a subject matter expert (SME) in various disciplines.
Must be able to identify opportunities for optimization of processes within the department or the plant.
Ability to work independently or in teams.

Physical / Safety Requirements:

Duties may require overtime work, including nights and weekends
Must be able to gown for Grade C environments
Use of hands and fingers to manipulate office equipment is required
Position requires sitting for long hours, but may involve walking or standing for periods of time.

In return, you'll be eligible for[1]:

Day One Benefits
- Medical & Dental Coverage
- Flexible Spending Accounts
- Life and AD&D Insurance
- Supplemental Life Insurance
  - Spouse Life Insurance
  - Child Life Insurance
- 401(k) Retirement Savings Plan with Company Match
- Time Off Program
  - Paid Holidays
  - Paid Time Off
  - Paid Parental Leave and more
- Adoption Reimbursement Program
- Education Assistance Program
- Employee Assistance Program
- Community and Volunteer Service Program
- Employee Ownership Plan
Additional Benefits
- Short and Long-Term Disability Insurance
- Voluntary Insurance Benefits
  - Vision Coverage
  - Accident
  - Critical Illness
  - Hospital Indemnity Insurance
  - Identity Theft Protection
  - Legal and more
- Onsite Campus Amenities
  - Workout Facility
  - Cafeteria
  - Credit Union

[1] Current benefit offerings are in effect through 12/31/26

Disclaimer

This job description is intended to provide the minimum knowledge, skills and abilities necessary to perform the job. It may not be inclusive of all the duties and responsibilities of the job. Simtra reserves the right to make modifications based on business requirements.

Equal Employment Opportunity

Simtra is proud to be an equal opportunity employer. Simtra evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.

Data Privacy

To learn more about Simtra's approach to data privacy, please review the Simtra Recruitment Platform Global Privacy Policy: https://simtra.com/privacy-policy/

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Refine Your Search

process validation associate iii jobs in bloomington, in

Process Validation Associate III

Quality Engineer III

Aseptic Manufacturing Risk Management Associate II

MSAT Senior Associate (Tech Transfer)

Packaging Validation Associate I - 1st Shift

Sterility Assurance Validation Associate I (1st shift)

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